Primary Device ID | 15694311110064 |
NIH Device Record Key | bfd58b80-0d8e-4bcf-8105-8fed311c963f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nox Filter Tube Connector |
Version Model Number | NOX-FTC50 |
Catalog Number | 552110 |
Company DUNS | 365741462 |
Company Name | Nox Medical ehf. |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com | |
Phone | 999-999-9999 |
support@noxmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15694311110064 [Primary] |
GS1 | 15694311111085 [Unit of Use] |
MNR | Ventilatory Effort Recorder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-16 |
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